2015
DOI: 10.1016/j.talanta.2015.06.053
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Reversible regulation of thrombin adsorption and desorption based on photoresponsive-aptamer modified gold nanoparticles

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Cited by 4 publications
(3 citation statements)
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“…13−15 The ability to incorporate molecular photoswitches into synthetic DNA sequences has opened up new possibilities for stimulus-responsive materials in these fields, 12,16−25 while at the same time enabling applications such as photoregulation of gene expression 26−28 and enzymatic reactions 29−31 and also facilitating studies of aptamer folding and target binding. 32,33 Perhaps the most widely used DNA photoswitch at present is based on azobenzene attached to the sugar−phosphate backbone during solid-phase DNA synthesis, as pioneered by Asanuma et al 34 When inserted into the phosphate backbone of a DNA via a D-threoninol linkage, the azobenzene intercalates with the neighboring nucleobase pairs through πstacking interactions and stabilizes the DNA duplex despite the distortion in the double helical structure. 35−37 Upon UV irradiation, trans-azobenzene converts to the nonplanar cis form, which destabilizes the duplex.…”
Section: ■ Introductionmentioning
confidence: 99%
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“…13−15 The ability to incorporate molecular photoswitches into synthetic DNA sequences has opened up new possibilities for stimulus-responsive materials in these fields, 12,16−25 while at the same time enabling applications such as photoregulation of gene expression 26−28 and enzymatic reactions 29−31 and also facilitating studies of aptamer folding and target binding. 32,33 Perhaps the most widely used DNA photoswitch at present is based on azobenzene attached to the sugar−phosphate backbone during solid-phase DNA synthesis, as pioneered by Asanuma et al 34 When inserted into the phosphate backbone of a DNA via a D-threoninol linkage, the azobenzene intercalates with the neighboring nucleobase pairs through πstacking interactions and stabilizes the DNA duplex despite the distortion in the double helical structure. 35−37 Upon UV irradiation, trans-azobenzene converts to the nonplanar cis form, which destabilizes the duplex.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Nucleic acids are now extensively used to design, tailor, and assemble nanomaterials ranging from Mirkin-type spherical nucleic acids to functional aptamers, DNA origami, and nanomachines. The ability to incorporate molecular photoswitches into synthetic DNA sequences has opened up new possibilities for stimulus-responsive materials in these fields, , while at the same time enabling applications such as photoregulation of gene expression and enzymatic reactions and also facilitating studies of aptamer folding and target binding. , …”
Section: Introductionmentioning
confidence: 99%
“…Azobenzene is an ideal photoresponsive molecule that is characteristic of trans -to- cis conversion upon irradiation with particular wavelengths of light (i.e., photoisomerization). Ultraviolet light, whose energy is comparable to the energy gap of the π–π* transition, can evoke trans -to- cis conversion of azobenzene, whereas blue light with energy equivalent to the n−π* transition is able to help its reverse cis -to- trans isomerization. As azobenzene is introduced into the paired bases of a DNA chain, the DNA duplex becomes photoresponsive. Very interestingly, visible-light irradiation has an insignificant impact on the chemical structure of DNA duplexes if azobenzene is in a trans form (a planar molecule), whereas the UV irradiation on trans -azobenzene can cause trans -to- cis conversion; then, the duplex would dissociate.…”
mentioning
confidence: 99%